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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839978Generated: October 30, 2026

Potassium Iodide → Diethyl 2-(5-acetoxypentyl)-2-methylmalonate

https://huagongshe.com/reaction/839978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDiethyl methylmalonateHCID 11857—
ReactantSodium hydrideHCID 24758—
Reactant1-Pentanol, 5-chloro-, 1-acetateHCID 88521—
SolventDimethylformamideHCID 6228—
ProductDiethyl 2-(5-acetoxypentyl)-2-methylmalonateHCID 54079282—

Reaction Steps

Sodium hydride (4.8 g., 0.2 mole) as a 50% suspension in mineral oil is washed with petroleum ether under nitrogen to remove the mineral oil, suspended in dry benzene (150 ml.), and the suspension cooled in an ice bath. Diethyl methylmalonate (34.8 g., 0.2 mole) dissolved in sieve dried DMF (150 ml.) is added to the suspension of sodium hydride dropwise. The mixture is allowed to stand overnight at room temperature. Potassium iodide (0.4 g.) and 5-acetoxypentyl chloride (32.9 g., 0.2 mole) are then added, and the mixture is heated for 24 hours at 125° in an oil bath. The reaction mixture is concentrated in vacuo, diluted with ether (200 ml.), and filtered to remove sodium chloride. The filtrate is washed with brine, dried over anhydrous magnesium sulfate and concentrated to yield 39.6 g. (66%) of oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04097504
Source datasetuspto-grants-1978_06
ORD IDord-787ca0568310422b854bd14a063b737c
Source noteuspto-grants-1978_06